Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature
Objective Fetal congenital cystic adenomatoid malformation (CCAM) is a rare lung abnormality with a highly variable prognosis depended on the presence of fetal hydrops and the size of the cysts. In case of fetal hydrops the prognosis is fatal without intervention. Methods and design Case report and...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Schott, Sarah [verfasserIn] Mackensen-Haen, Susanne [verfasserIn] Wallwiener, Markus [verfasserIn] Meyberg-Solomayer, Gabriele [verfasserIn] Kagan, Karl Oliver [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2008 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Archives of gynecology and obstetrics - Berlin : Springer, 1870, 280(2008), 2 vom: 20. Dez., Seite 293-296 |
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| Übergeordnetes Werk: |
volume:280 ; year:2008 ; number:2 ; day:20 ; month:12 ; pages:293-296 |
| Links: |
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| DOI / URN: |
10.1007/s00404-008-0880-4 |
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| Katalog-ID: |
SPR005099609 |
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| 100 | 1 | |a Schott, Sarah |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature |
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| 520 | |a Objective Fetal congenital cystic adenomatoid malformation (CCAM) is a rare lung abnormality with a highly variable prognosis depended on the presence of fetal hydrops and the size of the cysts. In case of fetal hydrops the prognosis is fatal without intervention. Methods and design Case report and literature review. Setting We report on the ultrasound and pathological findings of a hydropic fetus due to a CCAM Type II at 22 weeks of gestation. Conclusions Congenital cystic adenomatoid malformation is a rare fetal lung disease with an excellent prognosis in the absence of fetal hydrops. CCAM associated with fetal hydrops carries a grave prognosis but survival rates of 70% can be achieved by thoraco-amniotic drainage in those with macrocystic lesions. | ||
| 650 | 4 | |a CCAM |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Echogenic lung |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Hydrops fetalis |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Prenatal |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Mackensen-Haen, Susanne |e verfasserin |4 aut | |
| 700 | 1 | |a Wallwiener, Markus |e verfasserin |4 aut | |
| 700 | 1 | |a Meyberg-Solomayer, Gabriele |e verfasserin |4 aut | |
| 700 | 1 | |a Kagan, Karl Oliver |e verfasserin |4 aut | |
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10.1007/s00404-008-0880-4 doi (DE-627)SPR005099609 (SPR)s00404-008-0880-4-e DE-627 ger DE-627 rakwb eng 610 ASE 44.92 bkl Schott, Sarah verfasserin aut Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Objective Fetal congenital cystic adenomatoid malformation (CCAM) is a rare lung abnormality with a highly variable prognosis depended on the presence of fetal hydrops and the size of the cysts. In case of fetal hydrops the prognosis is fatal without intervention. Methods and design Case report and literature review. Setting We report on the ultrasound and pathological findings of a hydropic fetus due to a CCAM Type II at 22 weeks of gestation. Conclusions Congenital cystic adenomatoid malformation is a rare fetal lung disease with an excellent prognosis in the absence of fetal hydrops. CCAM associated with fetal hydrops carries a grave prognosis but survival rates of 70% can be achieved by thoraco-amniotic drainage in those with macrocystic lesions. CCAM (dpeaa)DE-He213 Echogenic lung (dpeaa)DE-He213 Hydrops fetalis (dpeaa)DE-He213 Prenatal (dpeaa)DE-He213 Mackensen-Haen, Susanne verfasserin aut Wallwiener, Markus verfasserin aut Meyberg-Solomayer, Gabriele verfasserin aut Kagan, Karl Oliver verfasserin aut Enthalten in Archives of gynecology and obstetrics Berlin : Springer, 1870 280(2008), 2 vom: 20. Dez., Seite 293-296 (DE-627)253390060 (DE-600)1458450-5 1432-0711 nnns volume:280 year:2008 number:2 day:20 month:12 pages:293-296 https://dx.doi.org/10.1007/s00404-008-0880-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.92 ASE AR 280 2008 2 20 12 293-296 |
| spelling |
10.1007/s00404-008-0880-4 doi (DE-627)SPR005099609 (SPR)s00404-008-0880-4-e DE-627 ger DE-627 rakwb eng 610 ASE 44.92 bkl Schott, Sarah verfasserin aut Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Objective Fetal congenital cystic adenomatoid malformation (CCAM) is a rare lung abnormality with a highly variable prognosis depended on the presence of fetal hydrops and the size of the cysts. In case of fetal hydrops the prognosis is fatal without intervention. Methods and design Case report and literature review. Setting We report on the ultrasound and pathological findings of a hydropic fetus due to a CCAM Type II at 22 weeks of gestation. Conclusions Congenital cystic adenomatoid malformation is a rare fetal lung disease with an excellent prognosis in the absence of fetal hydrops. CCAM associated with fetal hydrops carries a grave prognosis but survival rates of 70% can be achieved by thoraco-amniotic drainage in those with macrocystic lesions. CCAM (dpeaa)DE-He213 Echogenic lung (dpeaa)DE-He213 Hydrops fetalis (dpeaa)DE-He213 Prenatal (dpeaa)DE-He213 Mackensen-Haen, Susanne verfasserin aut Wallwiener, Markus verfasserin aut Meyberg-Solomayer, Gabriele verfasserin aut Kagan, Karl Oliver verfasserin aut Enthalten in Archives of gynecology and obstetrics Berlin : Springer, 1870 280(2008), 2 vom: 20. Dez., Seite 293-296 (DE-627)253390060 (DE-600)1458450-5 1432-0711 nnns volume:280 year:2008 number:2 day:20 month:12 pages:293-296 https://dx.doi.org/10.1007/s00404-008-0880-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.92 ASE AR 280 2008 2 20 12 293-296 |
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10.1007/s00404-008-0880-4 doi (DE-627)SPR005099609 (SPR)s00404-008-0880-4-e DE-627 ger DE-627 rakwb eng 610 ASE 44.92 bkl Schott, Sarah verfasserin aut Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Objective Fetal congenital cystic adenomatoid malformation (CCAM) is a rare lung abnormality with a highly variable prognosis depended on the presence of fetal hydrops and the size of the cysts. In case of fetal hydrops the prognosis is fatal without intervention. Methods and design Case report and literature review. Setting We report on the ultrasound and pathological findings of a hydropic fetus due to a CCAM Type II at 22 weeks of gestation. Conclusions Congenital cystic adenomatoid malformation is a rare fetal lung disease with an excellent prognosis in the absence of fetal hydrops. CCAM associated with fetal hydrops carries a grave prognosis but survival rates of 70% can be achieved by thoraco-amniotic drainage in those with macrocystic lesions. CCAM (dpeaa)DE-He213 Echogenic lung (dpeaa)DE-He213 Hydrops fetalis (dpeaa)DE-He213 Prenatal (dpeaa)DE-He213 Mackensen-Haen, Susanne verfasserin aut Wallwiener, Markus verfasserin aut Meyberg-Solomayer, Gabriele verfasserin aut Kagan, Karl Oliver verfasserin aut Enthalten in Archives of gynecology and obstetrics Berlin : Springer, 1870 280(2008), 2 vom: 20. Dez., Seite 293-296 (DE-627)253390060 (DE-600)1458450-5 1432-0711 nnns volume:280 year:2008 number:2 day:20 month:12 pages:293-296 https://dx.doi.org/10.1007/s00404-008-0880-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.92 ASE AR 280 2008 2 20 12 293-296 |
| allfieldsGer |
10.1007/s00404-008-0880-4 doi (DE-627)SPR005099609 (SPR)s00404-008-0880-4-e DE-627 ger DE-627 rakwb eng 610 ASE 44.92 bkl Schott, Sarah verfasserin aut Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Objective Fetal congenital cystic adenomatoid malformation (CCAM) is a rare lung abnormality with a highly variable prognosis depended on the presence of fetal hydrops and the size of the cysts. In case of fetal hydrops the prognosis is fatal without intervention. Methods and design Case report and literature review. Setting We report on the ultrasound and pathological findings of a hydropic fetus due to a CCAM Type II at 22 weeks of gestation. Conclusions Congenital cystic adenomatoid malformation is a rare fetal lung disease with an excellent prognosis in the absence of fetal hydrops. CCAM associated with fetal hydrops carries a grave prognosis but survival rates of 70% can be achieved by thoraco-amniotic drainage in those with macrocystic lesions. CCAM (dpeaa)DE-He213 Echogenic lung (dpeaa)DE-He213 Hydrops fetalis (dpeaa)DE-He213 Prenatal (dpeaa)DE-He213 Mackensen-Haen, Susanne verfasserin aut Wallwiener, Markus verfasserin aut Meyberg-Solomayer, Gabriele verfasserin aut Kagan, Karl Oliver verfasserin aut Enthalten in Archives of gynecology and obstetrics Berlin : Springer, 1870 280(2008), 2 vom: 20. Dez., Seite 293-296 (DE-627)253390060 (DE-600)1458450-5 1432-0711 nnns volume:280 year:2008 number:2 day:20 month:12 pages:293-296 https://dx.doi.org/10.1007/s00404-008-0880-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.92 ASE AR 280 2008 2 20 12 293-296 |
| allfieldsSound |
10.1007/s00404-008-0880-4 doi (DE-627)SPR005099609 (SPR)s00404-008-0880-4-e DE-627 ger DE-627 rakwb eng 610 ASE 44.92 bkl Schott, Sarah verfasserin aut Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Objective Fetal congenital cystic adenomatoid malformation (CCAM) is a rare lung abnormality with a highly variable prognosis depended on the presence of fetal hydrops and the size of the cysts. In case of fetal hydrops the prognosis is fatal without intervention. Methods and design Case report and literature review. Setting We report on the ultrasound and pathological findings of a hydropic fetus due to a CCAM Type II at 22 weeks of gestation. Conclusions Congenital cystic adenomatoid malformation is a rare fetal lung disease with an excellent prognosis in the absence of fetal hydrops. CCAM associated with fetal hydrops carries a grave prognosis but survival rates of 70% can be achieved by thoraco-amniotic drainage in those with macrocystic lesions. CCAM (dpeaa)DE-He213 Echogenic lung (dpeaa)DE-He213 Hydrops fetalis (dpeaa)DE-He213 Prenatal (dpeaa)DE-He213 Mackensen-Haen, Susanne verfasserin aut Wallwiener, Markus verfasserin aut Meyberg-Solomayer, Gabriele verfasserin aut Kagan, Karl Oliver verfasserin aut Enthalten in Archives of gynecology and obstetrics Berlin : Springer, 1870 280(2008), 2 vom: 20. Dez., Seite 293-296 (DE-627)253390060 (DE-600)1458450-5 1432-0711 nnns volume:280 year:2008 number:2 day:20 month:12 pages:293-296 https://dx.doi.org/10.1007/s00404-008-0880-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.92 ASE AR 280 2008 2 20 12 293-296 |
| language |
English |
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Enthalten in Archives of gynecology and obstetrics 280(2008), 2 vom: 20. Dez., Seite 293-296 volume:280 year:2008 number:2 day:20 month:12 pages:293-296 |
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Enthalten in Archives of gynecology and obstetrics 280(2008), 2 vom: 20. Dez., Seite 293-296 volume:280 year:2008 number:2 day:20 month:12 pages:293-296 |
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findex.gbv.de |
| topic_facet |
CCAM Echogenic lung Hydrops fetalis Prenatal |
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610 |
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false |
| container_title |
Archives of gynecology and obstetrics |
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Schott, Sarah @@aut@@ Mackensen-Haen, Susanne @@aut@@ Wallwiener, Markus @@aut@@ Meyberg-Solomayer, Gabriele @@aut@@ Kagan, Karl Oliver @@aut@@ |
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2008-12-20T00:00:00Z |
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253390060 |
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3610 |
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SPR005099609 |
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englisch |
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| author |
Schott, Sarah |
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Schott, Sarah ddc 610 bkl 44.92 misc CCAM misc Echogenic lung misc Hydrops fetalis misc Prenatal Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature |
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610 ASE 44.92 bkl Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature CCAM (dpeaa)DE-He213 Echogenic lung (dpeaa)DE-He213 Hydrops fetalis (dpeaa)DE-He213 Prenatal (dpeaa)DE-He213 |
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ddc 610 bkl 44.92 misc CCAM misc Echogenic lung misc Hydrops fetalis misc Prenatal |
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ddc 610 bkl 44.92 misc CCAM misc Echogenic lung misc Hydrops fetalis misc Prenatal |
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Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature |
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Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature |
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Schott, Sarah |
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Archives of gynecology and obstetrics |
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Schott, Sarah Mackensen-Haen, Susanne Wallwiener, Markus Meyberg-Solomayer, Gabriele Kagan, Karl Oliver |
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Schott, Sarah |
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10.1007/s00404-008-0880-4 |
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verfasserin |
| title_sort |
cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature |
| title_auth |
Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature |
| abstract |
Objective Fetal congenital cystic adenomatoid malformation (CCAM) is a rare lung abnormality with a highly variable prognosis depended on the presence of fetal hydrops and the size of the cysts. In case of fetal hydrops the prognosis is fatal without intervention. Methods and design Case report and literature review. Setting We report on the ultrasound and pathological findings of a hydropic fetus due to a CCAM Type II at 22 weeks of gestation. Conclusions Congenital cystic adenomatoid malformation is a rare fetal lung disease with an excellent prognosis in the absence of fetal hydrops. CCAM associated with fetal hydrops carries a grave prognosis but survival rates of 70% can be achieved by thoraco-amniotic drainage in those with macrocystic lesions. |
| abstractGer |
Objective Fetal congenital cystic adenomatoid malformation (CCAM) is a rare lung abnormality with a highly variable prognosis depended on the presence of fetal hydrops and the size of the cysts. In case of fetal hydrops the prognosis is fatal without intervention. Methods and design Case report and literature review. Setting We report on the ultrasound and pathological findings of a hydropic fetus due to a CCAM Type II at 22 weeks of gestation. Conclusions Congenital cystic adenomatoid malformation is a rare fetal lung disease with an excellent prognosis in the absence of fetal hydrops. CCAM associated with fetal hydrops carries a grave prognosis but survival rates of 70% can be achieved by thoraco-amniotic drainage in those with macrocystic lesions. |
| abstract_unstemmed |
Objective Fetal congenital cystic adenomatoid malformation (CCAM) is a rare lung abnormality with a highly variable prognosis depended on the presence of fetal hydrops and the size of the cysts. In case of fetal hydrops the prognosis is fatal without intervention. Methods and design Case report and literature review. Setting We report on the ultrasound and pathological findings of a hydropic fetus due to a CCAM Type II at 22 weeks of gestation. Conclusions Congenital cystic adenomatoid malformation is a rare fetal lung disease with an excellent prognosis in the absence of fetal hydrops. CCAM associated with fetal hydrops carries a grave prognosis but survival rates of 70% can be achieved by thoraco-amniotic drainage in those with macrocystic lesions. |
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Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature |
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https://dx.doi.org/10.1007/s00404-008-0880-4 |
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Mackensen-Haen, Susanne Wallwiener, Markus Meyberg-Solomayer, Gabriele Kagan, Karl Oliver |
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Mackensen-Haen, Susanne Wallwiener, Markus Meyberg-Solomayer, Gabriele Kagan, Karl Oliver |
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| doi_str |
10.1007/s00404-008-0880-4 |
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2024-07-03T13:59:30.923Z |
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| score |
7.3989916 |